Combined immunodeficiency due to ITK deficiency

Orpha code: 538963OMIM code: 613011

Definition

A rare autosomal recessive primary immunodeficiency characterized by susceptibility to Epstein-Barr virus (EBV)-associated lymphoproliferative disorders such as malignant B-cell proliferation, Hodgkin lymphoma, B-cell lymphoma, lymphoid granulomatosis, hemophagocytic lymphohistiocytosis, and smooth muscle tumor. Patients present persistent symptoms of infectious mononucleosis including recurrent febrile episodes, lymphadenopathies, and hepatosplenomegaly, accompanied by high EBV viral load in the blood. Additional manifestations are autoimmune diseases like hemolytic anemia or renal disease.

Disease data
Classification

Disease

Synonyms
Autosomal recessive lymphoproliferative disease due to ITK deficiency
Autosomal recessive lymphoproliferative disease due to ITK deficiency
ITK deficiency
ORPHA code
538963
OMIM code
613011
ICD10 code
D82.3
ICD11 code
-

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl